Product Details

SNP ID
rs10087720
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:36787414 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTTGCTTTCAGCCCAGACCTTTGTG[C/G]GGCAAGTGTTGGTAAGTACATTTTC
Phenotype
MIM: 615215
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
KCNU1 PubMed Links

Gene Details

Gene
KCNU1
Gene Name
potassium calcium-activated channel subfamily U member 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001031836.2 391 Missense Mutation CGG,GGG R102G NP_001027006.2
XM_011544424.1 391 Missense Mutation CGG,GGG R102G XP_011542726.1
XM_011544426.1 391 Missense Mutation CGG,GGG R102G XP_011542728.1
XM_011544427.1 391 Missense Mutation CGG,GGG R102G XP_011542729.1
XM_017013144.1 391 Missense Mutation CGG,GGG R102G XP_016868633.1

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